ENST00000248633.9:c.1516T=
MANE Select
|
ENSP00000248633.4:p.Ser506=
|
|
ENST00000248633.8:c.1516T=
|
ENSP00000248633.4:p.Ser506=
|
|
ENST00000422866.1:c.417T=
|
|
|
ENST00000428214.5:c.1516T=
|
ENSP00000394413.1:p.Ser506=
|
|
ENST00000438045.5:c.550T=
|
ENSP00000410438.1:p.Ser184=
|
|
ENST00000476923.1:n.277T=
|
|
|
ENST00000484913.5:n.1555T=
|
|
|
NM_000466.2:c.1516T=
|
NP_000457.1:p.Ser506=
|
|
NM_001282677.1:c.1516T=
|
NP_001269606.1:p.Ser506=
|
|
NM_001282678.1:c.892T=
|
NP_001269607.1:p.Ser298=
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|
XM_005250433.3:c.-151T=
|
XP_005250490.1:n.-151T=
|
|
XR_242246.3:n.1612T=
|
|
|
XM_017012319.2:c.-151T=
|
XP_016867808.1:n.-151T=
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|
XR_001744808.2:n.626T=
|
|
|
XR_242246.5:n.1563T=
|
|
|
NM_000466.3:c.1516T=
MANE Select
|
NP_000457.1:p.Ser506=
|
|
NM_001282677.2:c.1516T=
|
NP_001269606.1:p.Ser506=
|
|
NM_001282678.2:c.892T=
|
NP_001269607.1:p.Ser298=
|
|